#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA2390447	F	Binding affinity to CRTh2 receptor (unknown origin) overexpressed in CHOK1 cell membranes assessed as dissociation half life at 10 X IC50 preincubated for 1 hr followed by 0.1 nM to 100 uM PGD2 and [35S]-GTPgammaS addition measured after 2 hrs by liquid scintillation counting analysis	Homo sapiens	3	ALA2384997	cell-based format	Scientific Literature
2.	ALA2390449	B	Inhibition of thromboxane A2 receptor (unknown origin) at 10 uM relative to control	Homo sapiens	7	ALA2384997	single protein format	Scientific Literature
3.	ALA2390450	B	Inhibition of DP1 receptor (unknown origin) at 10 uM relative to control	Homo sapiens	7	ALA2384997	single protein format	Scientific Literature
4.	ALA2390453	A	Oral bioavailability in rat at 10 mg/kg	Rattus norvegicus	1	ALA2384997	organism-based format	Scientific Literature
5.	ALA2390454	A	Volume of distribution at steady state in rat at 1 mg/kg, iv	Rattus norvegicus	1	ALA2384997	organism-based format	Scientific Literature
6.	ALA2390455	A	Clearance in rat at 1 mg/kg, iv	Rattus norvegicus	1	ALA2384997	organism-based format	Scientific Literature
7.	ALA2390456	A	Terminal half life in rat at 1 mg/kg, iv	Rattus norvegicus	1	ALA2384997	organism-based format	Scientific Literature
8.	ALA2390607	A	AUC ( 0 to 24 hrs) in rat at 1 mg/kg, iv	Rattus norvegicus	1	ALA2384997	organism-based format	Scientific Literature
9.	ALA2390608	A	Plasma protein binding in human by rapid equilibrium dialysis method	Homo sapiens	1	ALA2384997	cell-free format	Scientific Literature
10.	ALA2390609	A	Plasma protein binding in rat by rapid equilibrium dialysis method	Rattus norvegicus	1	ALA2384997	cell-free format	Scientific Literature
11.	ALA2390614	P	Lipophilicity , log D of the compound at pH 7.4 by shake-flask method		2	ALA2384997	small-molecule physicochemical format	Scientific Literature
12.	ALA2390616	P	Solubility of the compound at pH 1		2	ALA2384997	small-molecule physicochemical format	Scientific Literature
13.	ALA2390617	P	Solubility of the compound at pH 7.4		2	ALA2384997	small-molecule physicochemical format	Scientific Literature
14.	ALA2390618	P	Dissociation constant, pKa of the compound by potentiometric method		2	ALA2384997	small-molecule physicochemical format	Scientific Literature
15.	ALA2390619	A	Apparent permeability from apical to basolateral side in human Caco2 cells	Homo sapiens	2	ALA2384997	cell-based format	Scientific Literature
16.	ALA2390620	A	Apparent permeability from basolateral to apical side in human Caco2 cells	Homo sapiens	2	ALA2384997	cell-based format	Scientific Literature
17.	ALA2390622	B	Antagonist activity at CRTh2 receptor in human whole blood assessed as inhibition of PGD2-induced eosinophil shape change preincubated for 10 mins followed by PGD2 addition measured after 4 mins by side scatter analysis	Homo sapiens	5	ALA2384997	single protein format	Scientific Literature
18.	ALA2390624	F	Antagonist activity at CRTh2 receptor (unknown origin) overexpressed in CHOK1 cell membranes assessed as inhibition of [35S]-GTPgammaS binding preincubated for 1 hr followed by 50 nM PGD2 and 0.1 nM [35S]-GTPgammaS addition measured after 2 hrs by liquid scintillation counting analysis	Homo sapiens	34	ALA2384997	cell-based format	Scientific Literature
19.	ALA3778970	B	Displacement of [35S]-GTPgammaS from CRTH2 receptor (unknown origin) expressed in CHOK1 cell membrane after 1 hr by liquid scintillation counter	Homo sapiens	22	ALA3774370	cell-based format	Scientific Literature
20.	ALA3778972	B	Antagonist activity at CRTH2 receptor (unknown origin) expressed in CHOK1 cells assessed as dissociation half life measured up to 25 hrs by GTPgammaS assay	Homo sapiens	26	ALA3774370	cell-based format	Scientific Literature